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Recombinant Human Superoxide dismutase [Mn], mitochondrial (SOD2)

ACP22110

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP22110 Target NameSOD2
Target Synonymsmitochondrial; Superoxide dismutase 2 mitochondrialFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range25-222
Protein LengthFull Length of Mature ProteinPurity>85% (SDS-PAGE)
Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP04179
Background Information
  • Uniprot Id

    P04179

  • Target Species

    Human

  • Target Name

    SOD2

  • Target Full Name

    Superoxide dismutase [Mn], mitochondrial

  • Target Function

    Destroys superoxide anion radicals which are normally produced within the cells and which are toxic to biological systems.

  • Target Involvement

    Microvascular complications of diabetes 6 (MVCD6)

  • Target Subcellular Location

    Mitochondrion matrix.

  • Target Protein Families

    Iron/manganese superoxide dismutase family

  • Target Synonyms

    Indophenoloxidase B; IPO B; IPOB; Manganese containing superoxide dismutase; Manganese SOD; Manganese superoxide dismutase; Mangano superoxide dismutase; Mn SOD; Mn superoxide dismutase; MNSOD; MVCD6; SOD 2; SOD2; SODM_HUMAN; Superoxide dismutase [Mn] mitochondrial; Superoxide dismutase [Mn], mitochondrial; Superoxide dismutase 2 mitochondrial

  • Target Background

    This gene is a member of the iron/manganese superoxide dismutase family. It encodes a mitochondrial protein that forms a homotetramer and binds one manganese ion per subunit. This protein binds to the superoxide byproducts of oxidative phosphorylation and converts them to hydrogen peroxide and diatomic oxygen. Mutations in this gene have been associated with idiopathic cardiomyopathy (IDC), premature aging, sporadic motor neuron disease, and cancer. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 1.

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